chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5133929860133929860G19GENIChomozygous128241337
5133929862133929862C20GENIChomozygous128241338
5133929866133929867T21GENIChomozygous128241339
5133929873133929873TCG20GENIChomozygous128241340
5133929874133929876AC20GENIChomozygous128241341
5133929891133929892G17GENIChomozygous128241342
5133929901133929902GA16GENIChomozygous114015172
5133929906133929907T18GENIChomozygous128241343
5133929910133929910A18GENIChomozygous128241344
5133929918133929919GA17GENIChomozygous118858407
5133929919133929920AG17GENIChomozygous118858408
5133929965133929966T19GENIChomozygous128241345
5133930008133930009G25GENIChomozygous128241346
5133930063133930063C24GENIChomozygous128241347
5133930089133930090C19GENIChomozygous128241348
5133930141133930142T15GENIChomozygous128241349
5133930201133930201T8GENIChomozygous128241350
5133930281133930281C4GENIChomozygous128241352
5133935176133935176A17GENIChomozygous130962524
5133937508133937514GCACCC21GENIChomozygous128241355
5133937827133937828TG21GENICpossibly homozygous114015177
5133939501133939502GT14GENIChomozygous126238925
5133941468133941469GA15GENIChomozygous126238926
5133943978133943979CT30GENIChomozygous126238927
5133944565133944565AAA23GENIChomozygous130962525
5133946622133946623TC19GENIChomozygous114015178
5133947231133947232TC24GENIChomozygous114015179
5133947627133947628TC16GENIChomozygous114015180
5133949507133949507TT12GENIChomozygous130962526
5133949653133949654AG26GENIChomozygous114015181
5133949654133949655AG26GENIChomozygous114015182
5133949656133949656TG26GENIChomozygous128241356
5133951146133951147AC23GENIChomozygous114015183
5133930292133930293TC5GENIChomozygous128300301
5133938834133938835AT14GENIChomozygous130971675
5133955044133955045GC13GENIChomozygous114015184
5133955661133955662GA19GENIChomozygous130971676
5133956582133956583GA20GENIChomozygous126238928
5133958043133958044GA21GENIChomozygous114015187
5133958727133958728TC16GENIChomozygous126238929
5133959105133959106CG4GENIChomozygous118845669